Introduction Brucella suis is the causative agent of brucellosis in suidae and is differentiated into five biovars (bv). Biovars 1 and 3 possess zoonotic potential and can infect humans, whereas biovar 2 represents the main source of brucellosis in feral and domestic pigs in Europe. Both aspects, the zoonotic threat and the economic loss, emphasize the necessity to monitor feral and domestic pig populations. Available serological or PCR based methods lack sensitivity and specificity.
Results Here a bioinformatics approach was used to identify a B. suis specific 17 bp repeat on chromosome II (BS1330_II0657 locus). This repeat is common for B. suis bv 1 to 4 and was used to develop a TaqMan probe assay. The average PCR efficiency was determined as 95% and the limit of detection as 12,5 fg/µl of DNA, equally to 3.7 bacterial genomes. This assay has the highest sensitivity of all previously described B. suis specific PCR assays, making it possible to detect 3-4 bacterial genomes per 1 µl of sample. The assay was tested 100% specific for B. suis and negative for other Brucella spp. and closely related non-Brucella species.
Conclusions This novel qPCR assay could become a rapid, inexpensive and reliable screening method for large sample pools of B. suis 1 to 4. This method will be applicable for field samples after validation.
- Disease surveillance
- Food safety
- Infectious diseases
- RT-PCR techniques
- Received August 19, 2014.
- Revision received January 30, 2015.
- Accepted February 11, 2015.
- Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions
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Brucellosis is a zoonotic infectious disease caused by different species of the genus Brucella. One of the prevalent species in feral pigs and hares is Brucella suis with five different biovars. The biovars (bv) 1–3 infect mainly suidae, bv 4 infects reindeers and bv 5 is rarely found in rodents (Alton and others 1988, Forbes 1991). All of them possess a zoonotic potential, but only bv 1 and 3 seem to cause severe diseases in humans (Munoz and others 2010). In Europe the most common cause of porcine brucellosis is due to infections with B. suis bv 2, whereas bv 1 and 3 are reported in Croatia only once (Garcia-Yoldi and others 2007, Cvetnic and others 2009). In most European countries feral pigs and hares seem to be the main reservoir for B. suis bv 2 (Garcia-Yoldi and others 2007, Leuenberger and others 2007, Melzer and others 2007, Munoz and others 2010, Gregoire and others 2012, Wu and others 2012). Transmission to domestic pigs may occur through direct contact, sexual transmission or shared water reservoirs (Risco and others 2014). The disease then causes infertility and abortion in female pigs and orchitis in male pigs. Furthermore, lymphadenitis, arthritis and subcutaneous abscesses may occur. Studies show that interactions between feral pigs and domestic pigs occur quite often (Wu and others 2012). Regarding the growing populations of feral pigs in Europe this could explain the increase of infections in domestic pigs with brucellosis since 1990 (Godfroid and Kasbohrer 2002). Therefore, brucellosis as a zoonotic disease is of great public health importance in many countries (Melzer and others 2007, Gerst and others 2010, Von Roost and others 2010). Monitoring of Brucella spp. infections in domestic livestock and wild animals is mainly based on detection of antibodies specific for smooth lipopolysaccharide. This includes the risk of false positive reactions, especially for porcine brucellosis due to cross-reacting antibodies to the highly similar O-antigen of Yersinia enterocolitica O:9 (Hurvell 1973). Additionally, non-reactors or animals which have not yet developed an antibody level can cause false negative results. During recent years PCR-based methods became more and more important as fast and reliable methods to detect Brucella-specific DNA from colony material or directly from field samples. On one hand conventional or real-time Brucella genus-specific PCR methods are used to identify brucellae from colony material or field samples (Bricker 2002, Probert and others 2004). On the other hand species-specific multiplex PCR techniques are implemented to differentiate on species level (Lopez-Goni and others 2011). Since real-time PCR is much more sensitive compared with conventional PCR it is often used to detect specific DNA in field samples directly. Obviously, a positive result in a genus-specific real-time PCR should be confirmed by a second method which ideally is a species-specific method. So far published real-time PCR methods are able to distinguish B. abortus, B. melitensis and B. suis bv 1 (Al Dahouk and others 2007a). In central Europe B. suis bv 2 is endemic in wild boar and hare populations and therefore influences monitoring of brucellosis at least in pig farms(Garcia-Yoldi and others 2007, Leuenberger and others 2007, Munoz and others 2010, Gregoire and others 2012, Wu and others 2012). The last outbreaks of brucellosis in pigs in Germany were B. suis bv 2 infections in outdoor holdings which have been confirmed by isolation of the infectious agent (Melzer and others 2007).
The aim of this study was to develop a quantitative real-time PCR (qPCR) assay as a sensitive diagnostic tool for detection of Brucella suis bv 1–4. These biovars are the most prevalent and are of special epidemiological importance.
Materials and methods
Bacterial strains and growth conditions
Bacteria used in this study are listed in Tables 1 and 2. A collection of 25 Brucella spp. reference strains, 75 B. suis field isolates and 30 closely related and clinically relevant non-Brucella species were obtained from the in house strain collection of the national reference laboratory for brucellosis (Friedrich-Loeffler-Institut, Germany). Brucella spp. strains were maintained on Brucella agar (Becton Dickinson) or Brucella agar, containing polymyxin B (2500 IE) bacitracin (12,500 IE), cyclohexymid (50 mg/l), nalidixic acid (2.5 mg/l), nystatin (50,000 IE) and vancomycin (10 mg/l), respectively (Farrell 1974). Brucella cultures were incubated with 5–10 per cent of CO2 at 37°C for 72 hours (Alton and others 1988). All other bacterial strains were routinely cultivated on 5 per cent sheep blood agar (Becton Dickinson) or Luria Bertani agar (Fisher Scientific) overnight at 37°C.
Preparation of DNA templates
DNA was extracted from single colonies and resuspended in 200 µl of sterile distilled water after heat inactivation for two hours at 80°C. DNA isolation was carried out using the HighPure PCR Template Preparation Kit (Roche Diagnostics, Mannheim, Germany) according to the manufacturer's instructions for bacteria. DNA quantity and purity was determined using a NanoDrop™ 1000 spectrophotometer (Thermo Fisher Scientific, Wilmington, USA). Serial 1:10 dilutions ranging from 100 ng to 1 fg/µl of DNA were prepared for qPCR efficiency and specificity testing. DNA was also directly isolated from one Brucella culture-positive spleen sample from a hare with the same extraction kit according to the manufacturer's instructions for mammalian tissue. This was done as an example to show suitability of this assay for field samples.
For identification of a B. suis-specific target whole genome alignments were performed using the Geneious software (Geneious 6.0.3, Biomatters Ltd., Auckland, New Zealand). Genome sequences from various Brucella spp. (Table 3) were obtained from the NCBI GenBank database and analysed for B. suis bv 1 and 2 conserved regions. Identified targets were then tested for specificity using BLAST search with a Discontiguous Megablast against the NCBI GenBank database.
Quantitative real time PCR
Oligonucleotides B. suis for 5′-GCC AAA TAT CCA TGC GGG AAG-3′ and B. suis rev 5′-TGG GCA TTC TCT ACG GTG TG-3′ targeting a 106 bp fragment of the BS1330_II0657 locus encoded on chromosome 2 of B. suis bv 1 with the FAM-labelled hydrolysis probe B. suis probe 6-carboxyfluorescein (FAM)-TTG CGC TTT TGT GAT CTT TGC GCT TTA TGG-BHQ1 were used for the qPCR detection assay (Jena Bioscience, Germany). Primer and probe were designed with Geneious software (Geneious 6.0.3, Biomatters Ltd., Auckland, New Zealand). For qPCR analysis the Stratagene Mx3000P QPCR System (Agilent Technologies, Santa Clara, USA) was used. The qPCR was performed in a 25 µl format using the 2× TaqMan Universal PCR Mastermix (Applied Biosystems, Foster City, California, USA), 0.3µM of each primer, 0.1µM probe and 2 µl of template DNA. The qPCR was carried out on an Mx3000P QPCR Instrument (Agilent Technologies, Santa Clara, California, USA) using the following cycling conditions: 50°C for 2 minutes, 95°C for 10 minutes and 50 cycles of 95°C for 15 seconds and 60°C for 1 minute. Data were analysed with the Mx3000Pro software. Raw data were normalised using an adaptive baseline correction and a smoothing with a moving average of three amplification points. Initially cycle threshold (Ct) was set with background-based threshold algorithm. For better comparison of the results a threshold of 0.05 (dRn) was applied to all qPCR signals, as the highest of all computed thresholds from all experiments. Fluorescence signals above this value were considered as positive, below as negative results.
Determination of qPCR efficiency
Standard curves were done with serial dilutions 1:10 from 106 to 100 fg/µl of bacterial DNA from B. suis bv 2. The efficiency of the PCR was calculated from the slope of the logarithmic regression of Ct values plotted against DNA concentrations by E=e(−1/slope)−1. For statistical analysis and assessment of reproducibility, standard curve experiments were done in quadruplicate and repeated five times on five different days. Additionally, qPCR efficiencies for B. suis bv 1–4 were compared by analysing serial dilutions 1:10 of genomic DNA from 106 to 102 fg/µl. Dilutions were chosen within the linear dynamic range of the assay and expected concentrations of DNA within possible specimens. Samples were analysed in duplicate.
Determination of the qPCR limit of detection
The limit of detection (LOD) was defined as the DNA concentration with 95 per cent positive qPCR results. Therefore we used 100, 50, 25, 12.5 and 6.25 fg/µl of B. suis bv 2 DNA spiked into DNA preparations from anti-Brucella antibody and Brucella DNA-free swine sera. To proof Brucella DNA free status of the sera a published real-time PCR (Probert and others 2004) was used as described. LOD samples were analysed in octuplicate for each concentration and repeated three times on three different days.
Capillary gel electrophoresis
Real time PCR products were analysed by capillary gel electrophoresis using the QIAxcel DNA high resolution kit (1200) with an analytical range of 15 bp to 10 kb on the QIAxcel Advanced system (QIAGEN, Hilden, Germany). Briefly, 10 µl of each PCR product were added to the template tray and a standardised volume of 0.1 μl was injected automatically into the QIAxcel cartridge for analysis. For accurate fragment size determination the QX alignment marker 15 bp/3 kb and the QX DNA size marker FX174/HaeIII with a range of 50–1350 bp was used. Electrophoresic separation of amplicons was then carried out by applying the OM500 program. For data analysis and generation of a virtual gel image the Biocalculator QIAxcel software was used.
Identification of a B. suis bv 1–4 specific qPCR target by whole genome comparison.
Annotated genome sequences from 12 Brucella spp. and B. suis bv 1 and 2 (Table 3) were analysed by whole genome comparison with B. suis bv 2 as reference genome. A region within the 3′ end of BS1330_II0657 locus was identified to be highly specific for B. suis with a 17 bp repeat exclusively found in B. suis bv 1–4 (Fig 1). All other Brucella spp. and B. suis bv 5 lack this repeat. Designed real-time primer were located up- and downstream of this repeat generating a 106 bp fragment for B. suis bv 1–4 and a 89 bp fragment for all other Brucella spp. and B. suis bv 5 (Fig 2). BLAST search performed for the 106 bp amplicon revealed 100 per cent complementarity for B. suis bv 1–4. The probe spanning the 17 bp repeat in B. suis bv 1–4 shows a 7 bp mismatch within the 5′-end in all other Brucella spp., lacking this repeat. However, this mismatch lowers the Tm to 57°C and prevents binding of the probe at the assay-specific annealing temperature of 60°C.
For PCR efficiency determination genomic DNA standards from 106 to 100 fg/µl of B. suis bv 2 DNA were analysed. Efficiency was calculated from the slope and ranged between 90.8 and 97.6 per cent with a y-interception between 38.88 and 40.15 and a R2 value between 0.9821 and 0.9965 (Fig 3). Analysis of B. suis bv 1, 3 and 4 DNA standards revealed similar efficiencies of 94.3–95.5 per cent with y-intercepts between Ct- value 44.24 and 45.24 and an R2 value between 0.9567 and 0.9965 (Fig 4). In general we observed a decreasing accuracy, assessed as an increasing standard error (se) for the resulting Ct values with decreasing DNA concentrations. The se increased from 1 ng/µl to 10 fg/µl from 0.20 to 0.83 during the PCR efficiency testing and from 100 fg/µl to 12.5 fg/µl from 0.36 to 1 for the LOD determination (Fig 5).
Limit of detection
The developed qPCR assay reproducibly detected 12.5 fg/µl of B. suis bv 2 DNA (3.7 bacterial genomes). At this DNA concentration all qPCR assays were 100 per cent positive. However, at a DNA concentration of 6.25 fg/µl (1.8 bacterial genomes), still 83 per cent of performed reactions were positive (Fig 5).
To evaluate the specificity of the B. suis qPCR, DNA preparations from 30 non-Brucella species (Table 1), 25 Brucella spp. reference strains including five B. suis reference strains (Table 1), representing all five biovars were tested at a concentration of 100 pg/µl. For all 30 non-Brucella species negative results were obtained with Ct values not exceeding the calculated y-intercept from qPCR efficiency testing of 40 for any DNA concentration used (data not shown). Similar results were obtained for all Brucella spp. analysed. Only DNA from B. suis bv 1–4 strains showed positive results with Ct values of approximately 22. There were no suspicious or undefined signals for non-B. suis bv 1–4 samples (Fig 6). Furthermore we analysed 75 field isolates (Table 2) from confirmed B. suis cases from various animal species and geographical regions which were all qPCR positive for B. suis bv 1–4. One sample, which was a confirmed human case of B. suis bv 5 was tested negative.
Isolated DNA of the true positive spleen sample from the field was tested positive by B. suis qPCR also.
The qPCR is a fast and reliable tool with still growing importance for direct detection of pathogens in clinical samples. For the diagnosis of brucellosis it has been already established and shown its usefulness. But till now and to the knowledge of the authors there is no description of a single probe qPCR that is able to detect all practically relevant B. suis bv 1–4. A test panel of overall 100 Brucella and 30 non-Brucella strains showed 100 per cent specificity of the new assay for B. suis bv 1–4. Our B. suis qPCR has an average efficiency of 95 per cent. This value shows its suitability for quantification of clinical samples even at very low concentrations of isolated DNA. A comparison of B. suis bv 1–4 showed no significant differences in Ct-values for a serial dilution 1:10 from 1 ng/µl to 1 pg/µl of DNA. For the efficiencies calculated from standard curves only B. suis bv 4 showed a decreased value of 88 per cent whereas B. suis bv 1–3 had efficiencies of 93–94.5 per cent.
The limit of detecting was set at a concentration of 12.5 fg/µl of template DNA. This means the assay is able to detect three to four bacterial genomes in 1 µl of DNA isolated from clinical samples. To our knowledge this is the highest sensitivity reached with a B. suis-specific qPCR assay (Redkar and others 2001, Bogdanovich and others 2004, Probert and others 2004, Al Dahouk and others 2007b, Fretin and others 2008). Nevertheless we observed an increased variance of Ct values for DNA concentrations of 100 fg/µl down to the LOD with 12.5 fg/µl. We think the only reason for this is the growing impact of dilution errors and the resulting variance of used DNA for a single qPCR reaction. By spiking DNA into eluates from negative swine sera we also showed that the assay could be useful for diagnosis of clinical samples. DNA directly isolated from tissue of a spleen sample of one, by isolation proofed Brucella infected hare, was tested positive in the B. suis qPCR. To use the method for clinical samples like sera or biopsy material a true validation procedure has to be done.
A real-time PCR based single nucleotide polymorphism analysis (Gopaul and others 2008) differentiates B. abortus, B. melitensis, B. ovis, B. suis, B. canis, B. neotomae and marine Brucella spp. but with lower sensitivity than what seems to be necessary to examine field samples.
Regarding the problems with specificity and sensitivity in serology and the insufficient limits of detecting in most qPCR assays, this new assay could play a key role in improving the performance of large-scale brucellosis screenings of wild boar or hare populations and surveillance in domestic pigs.
The authors gratefully thank Nadine Lemser, Michaela Ganß, Peggy Marten and Oda Schneider for excellent technical assistance.
- Received August 19, 2014.
- Revision received January 30, 2015.
- Accepted February 11, 2015.
Funding This research received no specific grant from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement No additional data are available.
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